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15449-66-8

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15449-66-8 Usage

General Description

Bicyclo[2.2.1]heptane-2,2-dimethanol, also known as norbornane-2,2-dimethanol, is a bicyclic organic compound with the molecular formula C9H16O2. It is a white, crystalline solid at room temperature and is soluble in water and organic solvents. This chemical is primarily used as a building block in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. It is also used as a chiral auxiliary in asymmetric synthesis and as a stabilizer in the production of plastic materials. Bicyclo[2.2.1]heptane-2,2-dimethanol has low toxicity and is considered to be non-hazardous when handled and stored properly.

Check Digit Verification of cas no

The CAS Registry Mumber 15449-66-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,4 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 15449-66:
(7*1)+(6*5)+(5*4)+(4*4)+(3*9)+(2*6)+(1*6)=118
118 % 10 = 8
So 15449-66-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H16O2/c10-5-9(6-11)4-7-1-2-8(9)3-7/h7-8,10-11H,1-6H2

15449-66-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-di-hydroxymethyl-norbornane

1.2 Other means of identification

Product number -
Other names 2,2-Dihydroxymethyl-norbornan

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:15449-66-8 SDS

15449-66-8Downstream Products

15449-66-8Relevant articles and documents

Tuning the Reactivity of Peroxo Anhydrides for Aromatic C-H Bond Oxidation

Pilevar, Afsaneh,Hosseini, Abolfazl,?ekutor, Marina,Hausmann, Heike,Becker, Jonathan,Turke, Kevin,Schreiner, Peter R.

, p. 10070 - 10079 (2018/09/06)

Phenol moieties are key structural motifs in many areas of chemical research from polymers to pharmaceuticals. Herein, we report on the design and use of a structurally demanding cyclic peroxide (spiro[bicyclo[2.2.1]heptane-2,4′-[1,2]dioxolane]-3′,5′-dione, P4) for the direct hydroxylation of aromatic substrates. The new peroxide benefits from high thermal stability and can be synthesized from readily available starting materials. The aromatic C-H oxidation using P4 exhibits generally good yields (up to 96%) and appreciable regioselectivities.

Hydroxyl-containing monomer, polymer, resist composition, and patterning process

-

Page/Page column 40-41, (2009/10/01)

A hydroxyl-containing monomer of formula (1) is provided wherein R1 is H, F, methyl or trifluoromethyl, R2 and R3 are monovalent C1-C15 hydrocarbon groups, or R2 and R3 may form an aliphatic ring. The monomers are useful for the synthesis of polymers which have high transparency to radiation of up to 500 nm and the effect of controlling acid diffusion so that the polymers may be used as a base resin to formulate radiation-sensitive resist compositions having a high resolution.

Treatment of neurodegenerative diseases

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, (2008/06/13)

Disclosed are methods for increasing the differentiation of mammalian neuronal cells for purposes of treating neurodegenerative diseases or nerve damage by administration of various compounds including alcohols, diols and/or triols and their analogues.

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